Borage Oil (Starflower Oil)

Borago officinalis
Evidence Level
Limited
2 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

Borage oil is cold-pressed from borage seeds (Borago officinalis, also known as 'starflower') — distinguished as having the highest known concentration of gamma-linolenic acid (GLA, ~20-26%) of any commercial plant oil, surpassing evening primrose (~9%) and black currant (~15%). Traditionally taken for skin, joint and premenstrual complaints, though the evidence has not held up evenly. A Cochrane review of 27 trials found oral borage and evening primrose oil are not effective for eczema, and the premenstrual and breast pain trials have also been null. The best supported use is as an add on in rheumatoid arthritis, and even there the trials used several times more GLA than a typical 1000 mg softgel provides. Critical: contains pyrrolizidine alkaloids (PAs) — hepatotoxic; reputable products are PA-tested/certified PA-free.

Studied Dose Consumer products supply 1-3 g borage oil a day, about 240-720 mg GLA. The rheumatoid arthritis trials used far more, 1.4 to 1.8 g GLA a day, roughly 6 to 8 g of oil.
Active Compound Gamma-linolenic acid (GLA, 20-26% of oil)

Benefits

Highest GLA Concentration of Plant Oils

Distinguishes borage from evening primrose (~9% GLA) and black currant (~15% GLA). Lower volume of borage oil needed for equivalent GLA dose. This is a statement about composition rather than a demonstrated health benefit. It means fewer capsules for the same GLA, not a better clinical result: no trial has shown borage oil to outperform evening primrose or black currant oil on any health outcome, and the one trial that compared borage seed oil head to head with fish oil in rheumatoid arthritis found no difference between them.

Rheumatoid Arthritis Adjunct

This is the best supported use and also the narrowest. Two placebo controlled trials in people with active rheumatoid arthritis reported reduced joint tenderness, swelling and morning stiffness: 37 patients on 1.4 g/day GLA from borage seed oil for 24 weeks, and 56 patients on 2.8 g/day GLA given as the purified free fatty acid for 6 months. A later 18 month trial in 150 patients compared borage seed oil, fish oil and the two combined; all three groups improved and none beat the others, but there was no placebo arm, so that trial cannot show the oil caused the improvement. A Cochrane review of herbal treatments for rheumatoid arthritis rated the pooled evidence for GLA oils as moderate for relieving pain and disability, while noting more adverse events on GLA than on placebo. Three limits matter. All of this work traces back to one research group, so none of it has been independently replicated. The doses correspond to roughly 6 to 12 g of oil a day, several times a standard 1000 mg softgel. And rheumatoid arthritis is a diagnosed autoimmune disease managed with prescription drugs: in the largest of these trials patients stayed on their usual arthritis medication at stable doses, so what was tested was borage oil added to standard treatment, never a substitute for it. The trial authors themselves wrote that GLA is not approved to treat any condition and should not be viewed as therapy for any disease.

Atopic Dermatitis / Eczema (Not Supported)

Earlier trials suggested benefit; larger systematic review of 27 trials found GLA (from borage and evening primrose) not effective for atopic dermatitis. Current consensus: no benefit despite long standing folk use. The Cochrane authors went further and judged the confidence intervals narrow enough that further eczema trials would be hard to justify. The two borage eczema trials cited on this page point the same way: a 160 patient, 24 week study found no overall efficacy on its primary outcome, and a 118 infant prevention trial found no significant effect on whether atopic dermatitis developed. Where borage oil does have measurable skin data is a different outcome in different people, namely dryness and barrier function in adults who do not have eczema. A 12 week placebo controlled study reported less water loss through the skin and less roughness and scaling, and a small uncontrolled study in older adults reported fewer complaints of dry skin. Both are small, neither has been replicated, and no trial has measured hair or nails at all.

Premenstrual Syndrome (Not Supported)

This is the weakest claim on the page and the evidence actually points the other way. Nearly all of it comes from evening primrose oil rather than borage, and the better trials are null: a review of the premenstrual syndrome trials concluded evening primrose oil is of little value, a 555 woman multicenter trial found GLA no better than placebo fatty acids for cyclic breast pain, and a 120 woman trial found evening primrose oil gave no clear benefit over control oils. No trial has tested borage oil itself for premenstrual symptoms. Treat this as an unsupported traditional use.

Diabetic Neuropathy (One Unreplicated Trial)

One multicentre trial in 111 people with mild diabetic neuropathy reported that 480 mg/day of GLA over a year moved all 16 nerve function and sensory measures in a more favourable direction than placebo, 13 of them significantly. That result has not been replicated in the decades since, the GLA was given as capsules rather than as borage oil, and no product built on it entered routine clinical use. Alpha lipoic acid has more consistent evidence for this indication. Diabetic neuropathy is a diagnosed complication of diabetes that needs medical management, so treat this as a historical research finding rather than a reason to self treat.

Mechanism of action

1

GLA → DGLA → PGE1 Anti-Inflammatory Pathway

GLA (gamma-linolenic acid) is metabolized via elongase to DGLA (dihomo-gamma-linolenic acid), which produces series-1 prostaglandins (PGE1) — anti-inflammatory, anti-platelet, vasodilatory. Distinguishes from arachidonic acid pathway producing pro-inflammatory PGE2. This is the biochemical rationale for the anti-inflammatory claims rather than evidence for them: the same pathway is why the eczema trials were run in the first place, and those trials were null.

2

Bypass Delta-6 Desaturase Limitation

Conversion of LA to GLA requires delta-6 desaturase — limited in: aging, diabetes, alcohol use, deficiency states. Direct GLA supplementation bypasses this conversion bottleneck. Theoretical advantage in those with reduced conversion capacity.

3

Skin Barrier Lipid Support

GLA contributes to skin barrier lipid composition. This is the one skin idea with supporting human measurements: oral supplementation lowered water loss through the skin and improved roughness and scaling in adult women over 12 weeks, and reduced complaints of dry skin in older adults. Those studies are small, one of them had no placebo group, and the same mechanism failed to produce any benefit in the eczema trials.

4

Cytokine Modulation

GLA modulates pro-inflammatory cytokine production (TNF-α, IL-1β, IL-6) via DGLA-derived eicosanoids and direct effects.

Clinical trials

1
Borage Oil for Rheumatoid Arthritis

Clinical trial of borage oil GLA (1.4 g GLA/day) vs placebo in 37 RA patients for 24 weeks.

37 RA patients.

GLA reduced tender joint count by 36 percent and swollen joint count by 28 percent versus placebo, while the placebo group showed no change or worsened, and no patient withdrew because of adverse effects. Context matters: this is a single trial of 37 people, run in the rheumatology clinic of a university hospital in patients already under specialist care, and the 1.4 g/day GLA dose corresponds to roughly 6 g of borage oil daily, six times a standard 1000 mg softgel. A later and larger trial from the same research group kept patients on their usual arthritis drugs at stable doses, which is how this should be read: an addition to standard treatment, never a replacement for DMARDs or biologics. The authors closed by writing that GLA is not approved for the treatment of any condition and should not be viewed as therapy for any disease.

2
GLA for Atopic Dermatitis — Evidence Review

Evidence review/pooled analysis of 27 clinical trials of borage and evening primrose oil for atopic dermatitis.

1,596 participants pooled across 27 randomized trials, 19 of evening primrose oil and 8 of borage oil.

GLA not effective for atopic dermatitis. Despite long folk use, clinical trial evidence does not support benefit. Notable example of folk medicine claims not surviving rigorous evaluation.

Side effects and drug interactions

Common Potential side effects

Generally well-tolerated.
Mild GI distress (nausea, soft stools).
Headache rare.
Pyrrolizidine alkaloid (PA) concern: the borage plant contains PAs that are toxic to the liver with repeated exposure. PA free is a marketing phrase with no single legal definition in the United States, so ask the seller for a certificate of analysis showing unsaturated pyrrolizidine alkaloids at or below the testing laboratory's limit of quantification. European risk assessors have proposed a tolerable daily intake for unsaturated PAs well under one microgram a day for an adult, which is how small the acceptable exposure is. Avoid untested oil, and avoid borage leaf teas and whole herb preparations, which carry far more PA than pressed seed oil does.
Seizure risk is unsettled but not purely theoretical: a 2011 case report describes status epilepticus in a patient who had been taking borage oil for a week. The older concern traces to evening primrose oil case reports from the early 1980s, which a 2007 review re-examined and concluded were a spurious association with the oil. The signal is weak in either direction, but anyone with a seizure disorder should clear borage oil with their prescriber before taking it.
Bleeding risk theoretical (modest).

Important Drug interactions

Anticoagulants and antiplatelet drugs: more than theoretical. The Cochrane eczema review cited on this page notes a study finding that evening primrose oil, the other common GLA oil, may increase bleeding in people taking warfarin. Tell your prescriber before combining.
Phenothiazines (chlorpromazine, prochlorperazine): these drugs lower the seizure threshold on their own, and a 2007 review concluded that the old evening primrose oil seizure reports were a spurious association with the oil. The interaction is therefore not well established, but given a separate case report of status epilepticus on borage oil, avoiding the combination remains the cautious choice.
Anticonvulsants — theoretical seizure risk; consult.
Hepatotoxic medications — pyrrolizidine alkaloid risk amplified; choose PA-tested products.
Pregnancy — limited safety data; PA risk for fetus; avoid without obstetric guidance.
Lactation — PAs may transfer to breast milk; avoid without medical guidance.
Pre-surgery — discontinue 1-2 weeks before.

Frequently asked questions about Borage Oil (Starflower Oil)

What is borage oil?

Borage oil is one of the richest sources of GLA (gamma-linolenic acid), an omega-6 fatty acid with anti-inflammatory properties. People take it for joint comfort and skin dryness. Worth knowing up front: the trials for eczema and for premenstrual symptoms were negative, so the marketed uses and the tested uses are not the same thing.

What is borage oil good for?

Its GLA has been studied most for joint comfort in rheumatoid arthritis, where two placebo controlled trials were positive at doses well above a normal softgel, though all of that work came from a single research group. The eczema evidence is negative: a Cochrane review of 27 trials found oral borage and evening primrose oil are not effective. Small studies suggest it may help plain dry skin and skin barrier function. Premenstrual and breast pain trials have been null, and there is no trial evidence for menopausal symptoms, hair or nails.

How much borage oil should I take?

Doses are based on GLA content, often providing around 240 to 1,000 mg of GLA per day. Follow product labeling, take it with food, and give it several weeks. Worth knowing: the rheumatoid arthritis trials used 1,400 to 2,800 mg of GLA per day, several times what a standard softgel provides, so a normal consumer dose is not the dose that was tested for joints.

Is borage oil safe?

It is generally well tolerated. Choose products certified free of pyrrolizidine alkaloids (natural compounds in borage that can harm the liver). It may have mild blood thinning activity, so check with your doctor if you take anticoagulants, and avoid it in pregnancy and while breastfeeding. There is also a case report of a seizure linked to borage oil, so anyone with a seizure disorder should ask their prescriber first.

What is Borage Oil used for?

Borage Oil is researched primarily for Hair, Skin & Nails and Joint Health. Distinguishes borage from evening primrose (~9% GLA) and black currant (~15% GLA). Lower volume of borage oil needed for equivalent GLA dose. This is a statement about composition rather than a demonstrated health benefit.

What is the recommended dosage of Borage Oil?

The clinically studied dose is Consumer products supply 1-3 g borage oil a day, about 240-720 mg GLA. The rheumatoid arthritis trials used far more, 1.4 to 1.8 g GLA a day, roughly 6 to 8 g of oil. Always follow the product label and check with a healthcare provider for personal advice.

Is Borage Oil safe, and does it have side effects?

For most healthy adults, Borage Oil is well tolerated at studied doses. Reported effects can include: Generally well-tolerated. Mild GI distress (nausea, soft stools). It may also interact with some medications. Borage Oil is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Borage Oil interact with any medications?

Possible interactions include: Anticoagulants and antiplatelet drugs: more than theoretical. The Cochrane eczema review cited on this page notes a study finding that evening primrose oil, the other common GLA oil, may increase bleeding in people taking warfarin. Tell your prescriber before combining. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Borage Oil?

NutraSmarts rates the evidence for Borage Oil as Limited (2 out of 5). It is backed by 2 clinical trials and 15 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(15 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Bamford JT, Ray S, Musekiwa A, van Gool C, Humphreys R, Ernst E. Oral evening primrose oil and borage oil for eczema. Cochrane Database Syst Rev. 2013;2013(4):CD004416. doi: 10.1002/14651858.CD004416.pub2.PubMedUsed to support: Systematic review of 27 randomized trials in 1,596 people, 8 of them using borage oil, testing oral evening primrose or borage oil for eczema. Neither oil improved global eczema symptoms compared with placebo, as rated either by patients or by doctors, and the reviewers judged the confidence intervals narrow enough that further trials would be hard to justify. This is why the skin section on this page does not claim an eczema benefit. One review author disclosed a past funding relationship with an evening primrose oil manufacturer, which if anything makes the negative conclusion harder to dismiss.
  2. Henz BM, Jablonska S, van de Kerkhof PC, Stingl G, Blaszczyk M, Vandervalk PG, Veenhuizen R, Muggli R, Raederstorff D. Double-blind, multicentre analysis of the efficacy of borage oil in patients with atopic eczema. Br J Dermatol. 1999;140(4):685-8. doi: 10.1046/j.1365-2133.1999.02771.x.PubMedUsed to support: Double blind multicenter trial in 160 adults with stable, moderate atopic eczema taking 500 mg of borage oil daily for 24 weeks, with topical steroid use as the primary measure. The overall response did not reach statistical significance, so the trial was negative on its main outcome. A benefit appeared only in a subgroup defined after the fact, created by excluding patients whose blood fatty acid levels showed they had not actually been taking the capsules. The 500 mg daily dose is also far below what the joint trials used.
  3. van Gool CJ, Thijs C, Henquet CJ, van Houwelingen AC, Dagnelie PC, Schrander J, Menheere PP, van den brandt PA. Gamma-linolenic acid supplementation for prophylaxis of atopic dermatitis--a randomized controlled trial in infants at high familial risk. Am J Clin Nutr. 2003;77(4):943-51. doi: 10.1093/ajcn/77.4.943.PubMedUsed to support: Double blind placebo controlled prevention trial in 118 formula fed infants with a maternal history of allergic disease, given borage oil supplying 100 mg of GLA daily for the first six months of life. It did not prevent atopic dermatitis and did not change total IgE at one year; severity showed only a trend in favor of GLA that did not reach significance. This is a prevention study in infants rather than a treatment study in adults, and it did not find a benefit.
  4. Zurier RB, Rossetti RG, Jacobson EW, DeMarco DM, Liu NY, Temming JE, White BM, Laposata M. gamma-Linolenic acid treatment of rheumatoid arthritis. A randomized, placebo-controlled trial. Arthritis Rheum. 1996;39(11):1808-17. doi: 10.1002/art.1780391106.PubMedUsed to support: Randomized placebo controlled trial in 56 patients with active rheumatoid arthritis, using 2.8 g/day of GLA as the purified free fatty acid against a sunflower seed oil placebo for 6 months, followed by a further 6 single blind months in which everyone received GLA. Meaningful improvement, defined as at least 25 percent better on four measures, occurred in 14 of 22 patients on GLA versus 4 of 19 on placebo. Two limitations matter here: the GLA was a purified fatty acid rather than borage oil, and 2.8 g of GLA is roughly what 12 g of borage oil would supply, far more than a standard softgel.
  5. Leventhal LJ, Boyce EG, Zurier RB. Treatment of rheumatoid arthritis with gammalinolenic acid. Ann Intern Med. 1993;119(9):867-73. doi: 10.7326/0003-4819-119-9-199311010-00001.PubMedUsed to support: Randomized double blind 24 week trial in 37 patients with active rheumatoid arthritis comparing 1.4 g/day of GLA in borage seed oil against cotton seed oil placebo, run in a university hospital rheumatology clinic. Tender joint count fell 36 percent and swollen joint count 28 percent, while the placebo group did not improve. This is the placebo controlled trial that used borage oil itself for joints, but it is small, and it shares a senior author with the other rheumatoid arthritis trials cited here, so none of them is an independent replication of the others. The dose corresponds to about 6 g of oil a day.
  6. Veselinovic M, Vasiljevic D, Vucic V, Arsic A, Petrovic S, Tomic-Lucic A, Savic M, Zivanovic S, Stojic V, Jakovljevic V. Clinical Benefits of n-3 PUFA and ɤ-Linolenic Acid in Patients with Rheumatoid Arthritis. Nutrients. 2017;9(4):. doi: 10.3390/nu9040325.PubMedUsed to support: Twelve week trial in 60 patients with active rheumatoid arthritis comparing fish oil, fish oil plus evening primrose oil, and no supplementation. Disease activity scores, tender joint counts and pain scores fell in both supplemented groups. Three limits make this weak support for borage oil specifically: the GLA came from evening primrose oil, it was given only together with fish oil so no separate GLA effect can be isolated, and the control group received nothing rather than a placebo, so the comparison was not blinded.
  7. Cameron M, Gagnier JJ, Chrubasik S Herbal therapy for treating rheumatoid arthritis. Cochrane Database Syst Rev. 2011;2011(2):CD002948..PubMedUsed to support: Systematic review of 22 randomized trials of herbal treatments for rheumatoid arthritis, including seven trials of GLA from evening primrose, borage or black currant seed oil. The reviewers found moderate evidence that these oils give some relief of pain and disability, and also recorded more adverse events on GLA than on placebo, roughly 20 percent versus 3 percent, a difference that was not statistically significant. Two limits for this page: the benefit is credited to GLA as a class rather than to borage oil specifically, and the pooled trials used doses well above a standard consumer softgel.
  8. De Spirt S, Stahl W, Tronnier H, et al. Intervention with flaxseed and borage oil supplements modulates skin condition in women. Br J Nutr. 2009;101(3):440-5..PubMedUsed to support: Twelve week randomized, placebo controlled study in women given 2.2 g/day of borage oil, the same amount of flaxseed oil, or a medium chain fat placebo, measuring ordinary skin condition rather than disease. Both oils reduced water loss through the skin and skin reddening and improved roughness and scaling; hydration rose on the oils but also in the placebo group, and no other measure moved on placebo. This is the honest basis for a dry skin and barrier claim, which is a different outcome from eczema, where borage oil failed. It is one small study in healthy volunteers, it has not been replicated, and it did not measure hair or nails.
  9. Brosche T, Platt D Effect of borage oil consumption on fatty acid metabolism, transepidermal water loss and skin parameters in elderly people. Arch Gerontol Geriatr. 2000;30(2):139-50..PubMedUsed to support: Two month study in 29 healthy older adults taking borage oil supplying 360 or 720 mg of GLA daily. Water loss through the skin fell by about 11 percent on average, complaints of dry skin dropped from 42 percent to 14 percent, and itching, reported by a third of the group at the start, was gone by the end. Two limitations matter: there was no placebo group, so improvement over time cannot be separated from the supplement, and instrument measured skin hydration did not change significantly even though the volunteers said their skin felt less dry.
  10. Keen H, Payan J, Allawi J, et al. Treatment of diabetic neuropathy with gamma-linolenic acid. The gamma-Linolenic Acid Multicenter Trial Group. Diabetes Care. 1993;16(1):8-15..PubMedUsed to support: One year randomized, double blind, placebo controlled multicentre trial in 111 patients with mild diabetic neuropathy given 480 mg/day of GLA. All 16 nerve function and sensory measures moved more favourably on GLA than on placebo, and 13 of those differences were statistically significant. This single trial is the entire basis for the diabetic neuropathy claim and it has stood alone since 1993: the GLA was given as capsules rather than as borage oil, the result has not been independently replicated, and diabetic neuropathy is a diagnosed complication of diabetes that needs medical management rather than self treatment.
  11. Budeiri D, Li Wan Po A, Dornan JC Is evening primrose oil of value in the treatment of premenstrual syndrome?. Control Clin Trials. 1996;17(1):60-8..PubMedUsed to support: Review of the placebo controlled trials of evening primrose oil for premenstrual syndrome, of which only seven existed and only five were clearly randomized. The two most rigorous trials showed no benefit, and the reviewers concluded the oil is of little value for premenstrual syndrome. It is cited here because the premenstrual claim made for borage oil is borrowed from evening primrose oil, and the borrowed evidence is negative.
  12. Goyal A, Mansel RE A randomized multicenter study of gamolenic acid (Efamast) with and without antioxidant vitamins and minerals in the management of mastalgia. Breast J. 2005;11(1):41-7..PubMedUsed to support: Double blind placebo controlled multicenter trial in 555 women with moderate to severe cyclic breast pain, testing GLA with and without antioxidant vitamins and minerals over four menstrual cycles. Pain improved in every arm including placebo, with about 40 percent responding on the placebo fatty acids, and GLA was no better than placebo whether or not the antioxidants were included. Cited to correct the cyclic mastalgia claim, which is borrowed from evening primrose oil rather than tested on borage oil, and which does not hold up.
  13. Blommers J, de Lange-De Klerk ES, Kuik DJ, et al. Evening primrose oil and fish oil for severe chronic mastalgia: a randomized, double-blind, controlled trial. Am J Obstet Gynecol. 2002;187(5):1389-94..PubMedUsed to support: Six month randomized double blind trial in 120 premenopausal women with severe chronic breast pain comparing evening primrose oil, fish oil, both, and control oils. Days with pain fell about 12 percent on evening primrose oil versus about 14 percent on its control oil, with no meaningful difference between them. A second independent negative result for the breast pain and premenstrual use, again in evening primrose oil rather than borage.
  14. Al-Khamees WA, Schwartz MD, Alrashdi S, et al. Status epilepticus associated with borage oil ingestion. J Med Toxicol. 2011;7(2):154-7..PubMedUsed to support: Case report of status epilepticus in a patient who had been taking borage oil for one week. A single case cannot establish cause and the report gives no dose, but it is the concrete basis for the seizure caution in the safety section, and it is more recent and more specific to borage oil than the 1980s evening primrose oil reports the caution is usually traced to.
  15. Reed GW, Leung K, Rossetti RG, et al. Treatment of rheumatoid arthritis with marine and botanical oils: an 18-month, randomized, and double-blind trial. Evid Based Complement Alternat Med. 2014;2014:857456..PubMedUsed to support: Eighteen month randomized double blind trial in 150 patients with rheumatoid arthritis comparing borage seed oil supplying 1.8 g/day of GLA, fish oil, and the two combined, on top of their usual arthritis drugs. Disease activity fell meaningfully in all three groups by 9 months and the improvement held to 18 months, with no difference between the groups, and participants reduced their prescription arthritis drugs more than matched registry patients did. The decisive limitation is that there was no placebo arm, by design, so the trial cannot show the oils caused the improvement; it also comes from the same research group as the two earlier trials cited here. It does answer one practical question: borage oil was studied alongside standard rheumatoid arthritis treatment, at stable doses, not instead of it.